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Syndromic genetic hearing loss
- Palmoplantar keratoderma with deafness is a disorder characterized by skin abnormalities and hearing loss. Affected individuals develop unusually thick skin on the ...
- Vohwinkel syndrome is a disorder with classic and variant forms, both of which affect the skin.In the classic form of Vohwinkel syndrome, affected individuals ...
- Keratitis-ichthyosis-deafness (KID) syndrome is characterized by eye problems, skin abnormalities, and hearing loss.People with KID syndrome usually have keratitis, ...
- Bart-Pumphrey syndrome is characterized by nail and skin abnormalities and hearing loss.People with Bart-Pumphrey syndrome typically have a white discoloration ...
- Hystrix-like ichthyosis with deafness (HID) is a disorder characterized by dry, scaly skin (ichthyosis) and hearing loss that is usually profound. Hystrix-like ...
- Hearing and Balance Symptoms and Conditions (American Academy of Audiology)Hearing Disorders and Deafness/Specifics ... Hearing Disorders and Deafness ... American Academy of Audiology ... Hearing and balance symptoms could be identifiers for ...
- Enlarged Vestibular Aqueduct (EVA) (Vestibular Disorders Association)Enlarged Vestibular Aqueduct is a condition caused by a malformation in the inner ear that leads to loss of hearing and vestibular function. ... Dizziness ...
- ... cell is sufficient to cause the disorder. JWS ... Agochukwu NB, Solomon BD, Muenke M. Hearing loss in syndromic craniosynostoses: otologic manifestations and clinical findings. Int J ...
- ... described as syndromic. The most common form of syndromic retinitis ... genetic syndromes, including Bardet-Biedl syndrome; Refsum disease; and ...
- ... associated with nonsyndromic hearing loss can also cause syndromic forms of ... to genetic changes, hearing loss can result from environmental factors ...